| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4678 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G/G | NA: NA |
| S4679 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G/A | NA: NA |
| S4680 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | A/A | NA: NA |
| S4681 | missense_variant | MTHFD1 | NM_005956.4:c.1958G>A | G/A+A/A | NA: NA |